@article {1429362,
	title = {Decoding reactive structures in dilute alloy catalysts},
	journal = {Nature Communications},
	volume = {13},
	year = {2022},
	pages = {1-9},
	abstract = {<section aria-labelledby="Abs1" data-gtm-vis-first-on-screen-50443292_562="513" data-gtm-vis-first-on-screen-50443292_563="513" data-gtm-vis-polling-id-50443292_562="130" data-gtm-vis-polling-id-50443292_563="131" data-gtm-vis-recent-on-screen-50443292_562="513" data-gtm-vis-recent-on-screen-50443292_563="513" data-gtm-vis-total-visible-time-50443292_562="6800" data-gtm-vis-total-visible-time-50443292_563="6800" data-title="Abstract" lang="en">
	<p>
		Rational catalyst design is crucial toward achieving more energy-efficient and sustainable catalytic processes. Understanding and modeling catalytic reaction pathways and kinetics require atomic level knowledge of the active sites. These structures often change dynamically during reactions and are difficult to decipher. A prototypical example is the hydrogen-deuterium exchange reaction catalyzed by dilute Pd-in-Au alloy nanoparticles. From a combination of catalytic activity measurements, machine learning-enabled spectroscopic analysis, and first-principles based kinetic modeling, we demonstrate that the active species are surface Pd ensembles containing only a few (from 1 to 3) Pd atoms. These species simultaneously explain the observed X-ray spectra and equate the experimental and theoretical values of the apparent activation energy. Remarkably, we find that the catalytic activity can be tuned on demand by controlling the size of the Pd ensembles through catalyst pretreatment. Our data-driven multimodal approach enables decoding of reactive structures in complex and dynamic alloy catalysts.
	</p>
</section>
},
	url = {https://www.nature.com/articles/s41467-022-28366-w},
	author = {Marcella, N and Lim, J S and Plonka, A M and Yan, G and Owen CJ and van der Hoeven, JES and Foucher, AC and Ngan, HT and Torrisi, SB and Marinkovic, NS and Stach, E.A. and Weaver, JF and Aizenberg, J and Sautet, P and Kozinsky, B and Frenkel, A}
}
